Canonical Allele Identifier: CA415108406

Gene: ABCD1

Linked Data

• dbSNP Id: rs868921503
• MyVariant Identifiers: chrX:g.153002652A>G (hg19) ; chrX:g.153737198A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153737198A>G , CM000685.2:g.153737198A>G	GRCh38
NC_000023.10:g.153002652A>G , CM000685.1:g.153002652A>G	GRCh37
NC_000023.9:g.152655846A>G	NCBI36
NG_009022.2:g.17331A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218104.6:c.1435A>G MANE Select	ENSP00000218104.3:p.Ile479Val
ENST00000218104.5:c.1435A>G	ENSP00000218104.3:p.Ile479Val
ENST00000443684.2:n.438A>G
NM_000033.3:c.1435A>G	NP_000024.2:p.Ile479Val
XR_938507.1:n.1907A>G
XR_938507.2:n.1907A>G
NM_000033.4:c.1435A>G MANE Select	NP_000024.2:p.Ile479Val